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EP3104700B1 - Emulgierbares konzentrat mit pestizid, fettsäureamid und lactamid - Google Patents

Emulgierbares konzentrat mit pestizid, fettsäureamid und lactamid Download PDF

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Publication number
EP3104700B1
EP3104700B1 EP15704994.1A EP15704994A EP3104700B1 EP 3104700 B1 EP3104700 B1 EP 3104700B1 EP 15704994 A EP15704994 A EP 15704994A EP 3104700 B1 EP3104700 B1 EP 3104700B1
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EP
European Patent Office
Prior art keywords
phenyl
methyl
formula
weight
chloro
Prior art date
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EP15704994.1A
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English (en)
French (fr)
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EP3104700A1 (de
Inventor
Murat Mertoglu
Stefan Bechtel
Natascha ANNAWALD
Marcus Annawald
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BASF Agro BV
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BASF Agro BV
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Priority to PL15704994T priority Critical patent/PL3104700T3/pl
Publication of EP3104700A1 publication Critical patent/EP3104700A1/de
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Classifications

    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
    • A01N43/647—Triazoles; Hydrogenated triazoles
    • A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
    • A01N25/04—Dispersions, emulsions, suspoemulsions, suspension concentrates or gels
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
    • A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
    • A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
    • A01N47/24—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing the groups, or; Thio analogues thereof

Definitions

  • Subject matter of the present invention is an emulsifiable concentrate comprising a water-insoluble pesticide, an amide of the formula (I) as defined herein, and a lactamide of the formula (II) as defined herein.
  • the invention further relates to a process for the preparation of said concentrate; an emulsion obtainable by mixing water, a water-insoluble pesticide, the amide of the formula (I) and the lactamide of the formula (II); and to a method for controlling phytopathogenic fungior undesired vegetation , where the concentrate or the emulsion is allowed to act on the soil or on undesired plants or on the crop plants and/or their environment.
  • Emulsifiable concentrates also referred to as EC are widely used formulations in crop protection.
  • WO 2013/087416 discloses emulsifiable concentrates of water-insoluble pesticides using fatty amides and hydrocarbons as solvent.
  • US 2007/270612 discloses emulsifiable concentrates of water-insoluble pesticides using fatty amides as solvent.
  • US 2013/210627 discloses emulsifiable concentrates of water-insoluble pesticides using lactamides and aromatic hydrocarbons inter alia as solvents.
  • the disadvantage of the known emulsifiable concentrates is the poor cold stability, the pronounced tendency to crystallize and the low pesticide concentration. It was an object of the present invention to provide an emulsifiable concentrate which overcomes these disadvantages.
  • the object was achieved by an emulsifiable concentrate comprising a water-insoluble pesticide, an amide of the formula (I) R 1 -C(O)N(R 2 ) 2 (I) where R 1 is C 5 -C 19 -alkyl and R 2 is methyl, ethyl, propyl, butyl, or mixtures thereof; and a lactamide of the formula (II) H 3 C-CH(OH)-C(O)N(R 3 ) 2 (II) where R 3 is methyl, ethyl, propyl, butyl, or mixtures thereof, wherein the pesticide is soluble in water to not more than 1 g/l at 25°C, wherein the concentrate comprises from 15% to 65% by
  • an emulsifiable concentrate is taken to mean compositions which form an oil-in-water emulsion upon mixing with water (e.g. in a weight ratio of 1 part concentrate to 99 parts water).
  • the emulsion usually arises spontaneously.
  • the resulting emulsion may have an average droplet size of more than 0.1 ⁇ m, preferably more than 0.5 ⁇ m, in particular more than 0.8 ⁇ m, and most preferred more than 1.1 ⁇ m.
  • the average droplet size may be determined by laser diffraction, e.g. with a Malvern Mastersizer 2000.
  • the concentrate is preferably present as a homogeneous solution. It is usually virtually free from dispersed particles.
  • Preferred amides of the formula (I) are those in which R 1 is C 7 -C 13 -alkyl (preferably linear) and R 2 is methyl.
  • Particular preferred amides of the formula (I) are those in which R 1 is C 7 -C 11 -alkyl and R 2 is methyl.
  • R 1 is n-nonyl and R 2 is methyl.
  • the amides of the formula (I) are those in which R 1 is C 8 -C 14 -alkyl, in particular linear C 8 -C 14 -alkyl.
  • Especially preferred amides of the formula (I) are those in which R 1 is C 7 -C 11 -alkyl, in particular linear C 7 -C 11 -alkyl. More particularly, R 1 is n-nonyl. Furthermore, it is preferred if R 2 is methyl.
  • Mixtures of amides of the formula (I) are also possible, for example mixtures where R 1 is C 7 -C 11 -alkyl and R 2 is methyl.
  • Mixtures of amides of the formula (I) comprise in most cases two amides of the formula (I) in an amount of in each case at least 30% by weight (preferably at least 40% by weight) based on the total amount of amides of the formula (I).
  • Preferred lactamides of the formula (II) are those in which R 3 is methyl.
  • R 3 is propyl or butyl, these alkyl groups may be linear or branched (e.g. iso-propyl, or tert-butyl).
  • the concentrate comprises from 1% to 30% by weight, more specifically from 3% to 30% by weight of the lactamide of the formula (II).
  • the weight ratio of the amide of the formula (I) to the lactamide of the formla (II) may be in the range from 1:2 to 15:1, more preferably from 1:1 to 13:1, and in particular from 2:1 to 11:1.
  • the concentrate may further comprise a hydrocarbon in addition to the amide of formula (I) and the lactamide of formula (II).
  • Suitable hydrocarbon solvents are aliphatic (such as linear or cyclic) or aromatic hydrocarbons.
  • Preferred hydrocarbon solvents are aromatic hydrocarbons.
  • Aromatic hydrocarbons may, besides at least one aromatic hydrocarbon unit, also comprise aliphatic hydrocarbon substituents.
  • the hydrocarbon solvent has a solubility in water of not more than 5% by weight, preferably not more than 1% by weight and in particular not more than 0.3% by weight at 20°C.
  • the hydrocarbon solvent has a boiling point at 1013 mbar of at least 100°C, preferably at least 150°C and in particular at least 180°C.
  • the hydrocarbon solvent comprises only carbon and hydrogen atoms.
  • the hydrocarbon solvent is preferably a C 6 -C 20 -hydrocarbon, in particular a C 8 -C 16 -hydrocarbon.
  • Suitable aromatic hydrocarbons are above all alkyl-substituted aromatics, such as toluene, the xylenes, ethylbenzenes and benzenes having longer-chain alkyl radicals, for example C 9 -C 10 -dialkyl- and -trialkylbenzenes (for example Solvesso® 100 from Exxon Mobile Europe or Aromatic 100 from Exxon Mobile USA), C 10 -C 11 -alkylbenzenes (for example Solvesso® 150 from Exxon Mobile Europe or Aromatic 150 from Exxon Mobile USA) and alkylnaphthalenes (for example Solvesso® 200 from Exxon Mobile Europe or Aromatic 200 from Exxon Mobile USA).
  • C 9 -C 10 -dialkyl- and -trialkylbenzenes for example Solvesso® 100 from Exxon Mobile Europe or Aromatic 100 from Exxon Mobile USA
  • the aromatic hydrocarbon comprises not more than 5% by weight, more preferably not more than 2% by weight and in particular not more than 1% by weight of naphthalene, based on the total weight of the aromatic solvent.
  • solvents with a naphthalene content of not more than 1% by weight are commercially available for example from Exxon Mobile Europe with the designation ND (naphthalene depleted), for example Solvesso® 150 ND and Solvesso® 200 ND from Exxon Mobile Europe. Even lower naphthalene contents of not more than 0.1% by weight are present in the products Aromatic 150 ULN and Aromatic 200 ULN from Exxon Mobile USA.
  • the concentrate comprises from 2% to 45% by weight, more specifically from 5% to 45% by weight of the hydrocarbon.
  • the concentrate comprises from 15 to 65% by weight of the amide of the formula (I), 1 to 30% by weight of the lactamide of the formula (II), and optionally 5 to 40% by weight of the hydrocarbon, wherein the amounts of these components add up to a sum of 16 to 90% by weight.
  • the concentrate is free from water.
  • the concentrate is essentially or largely, respectively, free from water. It can comprise not more than 3% by weight, preferably not more than 1% by weight of water.
  • the concentrate may comprise not more than 0.5% by weight of water. In a special form, the concentrate may comprise not more than 0.3% by weight and in particular not more than 0.1% by weight of water.
  • the concentrate may comprise further solvents (e.g. the organic solvents listed below) in addition the amide of the formula (I), the lactamide of the formula (II) and the hydrocarbon.
  • the concentrate can comprise not more than 30% by weight, preferably not more than 10% by weight. In a particular embodiment, it comprises not more than 1% by weight of the further solvents.
  • the pesticide is present in dissolved form, the concentrate is largely free from water and the concentrate present as a homogeneous solution.
  • pesticide refers to at least one active substance selected from the group of the fungicides, insecticides, nematicides, herbicides, safeners, biopesticides and/or growth regulators.
  • Preferred pesticides are fungicides, insecticides, herbicides and growth regulators.
  • Especially preferred pesticides are fungicides.
  • Mixtures of pesticides of two or more of the abovementioned classes may also be used. The skilled worker is familiar with such pesticides, which can be found, for example, in the Pesticide Manual, 16th Ed. (2013), The British Crop Protection Council, Lond on.
  • the following classes A) to K) refer to fungicides.
  • the pesticide is selected from the class B) Sterol biosynthesis inhibitors (SBI fungicides), more particularly selected from C14 demethylase inhibitors (DMI fungicides).
  • SBI fungicides Sterol biosynthesis inhibitors
  • DMI fungicides C14 demethylase inhibitors
  • the pesticide is selected from the group of triazole fungicides, more specifically is a compound of the following formula: wherein
  • the pesticide is selected from the triazoles I-1 to I-31:
  • the pesticide is selected from the compounds I-1, I-2, I-3, I-4, I-5, 1-14 and I-19.
  • the pesticide is selected from the compounds I-1, I-3, I-4, I-5 and I-19.
  • the pesticide is selected from the compounds I-1, I-3, I-5 and I-19.
  • the pesticide is selected from the compounds I-1, I-3 and I-5. In one embodiment, it is I-1, in a further embodiment, it is I-3. In still another embodiment, it is I-5.
  • the triazole fungicides of formula I in particular I-1 to I-31, are known as fungicides. They can be obtained by various routes in analogy to prior art processes known (cf. J.Agric. Food Chem. (2009) 57, 4854-4860 ; EP 0 275 955 A1 ; DE 40 03 180 A1 ; EP 0 113 640 A2 ; EP 0 126 430 A2 ).
  • the compounds I comprise chiral centers and they may be obtained in the form of racemates.
  • the R- and S-enantiomers of the triazole compounds can be separated and isolated in pure form with methods known by the skilled person, e.g. by using chiral HPLC. Suitable for use are both the enantiomers and compositions thereof.
  • said compounds I can be present in different crystal modifications, which may differ in biological activity.
  • any proportions of the (R)-enantiomer and the (S)-enantiomer of the respective compound I-1, I-2, I-3, I-4, I-5, etc., respectively, may be present.
  • the (R)-enantiomer of compound I-3 is (R)-2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-1-(1,2,4-triazol-1-yl)propan-2-ol
  • the (S)-enantiomer of I-3 is (S)-2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-1-(1,2,4-triazol-1-yl)propan-2-ol. This applies to the other compounds accordingly.
  • the respective compound I-1, I-2, I-3, I-4 or I-5, respectively, etc. may be provided and used as (R)-enantiomer with an enantiomeric excess (e.e.), e.g. of at least 40%, for example, at least 50%, 60%, 70% or 80%, preferably at least 90%, more preferably at least 95%, yet more preferably at least 98% and most preferably at least 99%.
  • an enantiomeric excess e.e.
  • the respective compound I is provided and used as (S)-enantiomer with an enantiomeric excess (e.e.) of at least 40%, for example, at least 50%, 60%, 70% or 80%, preferably at least 90%, more preferably at least 95%, yet more preferably at least 98% and most preferably at least 99%. This applies to every composition detailed herein.
  • the pesticides that may be also used according to the invention, their preparation and their biological activity e. g. against harmful fungi, pests or weed is known (cf.: http://www.alanwood.net/pesticides/); these substances are mostly commercially available.
  • the pesticide is selected from the group of the Inhibitors of complex III at Q o site (e.g. strobilurins).
  • the pesticide is selected from the group consisting of azoxystrobin, coumethoxystrobin, coumoxystrobin, dimoxystrobin, enestroburin, fenaminstrobin, fenoxystrobin/flufenoxystrobin, fluoxastrobin, kresoxim-methyl, metominostrobin, orysastrobin, picoxystrobin, pyraclostrobin, pyrametostrobin, pyraoxystrobin, trifloxystrobin, 2-[2-(2,5-dimethyl-phenoxymethyl)-phenyl]-3-methoxy-acrylic acid methyl ester, 2-(2-(3-(2,6-dichlorophenyl)-1-methyl-allylideneaminooxymethyl)-phenyl)-2-methoxyimino-N-methyl-acetamide, pyribencarb, triclopyricarb/chlorodincarb, famoxadone and f
  • the pesticide is selected from the group of the inhibitors of complex II (e. g. carboxamides).
  • the pesticide is selected from the group consisting of benodanil, benzovindiflupyr, bixafen, boscalid, carboxin, fenfuram, fluopyram, flutolanil, fluxapyroxad, furametpyr, isofetamid, isopyrazam, mepronil, oxycarboxin, penflufen, penthiopyrad, sedaxane, tecloftalam, thifluzamide, N-(4'-trifluoromethylthiobiphenyl-2-yl)-3-difluoromethyl-1-methyl-1H-pyrazole-4-carboxamide, N-(2-(1,3,3-trimethyl-butyl)-phenyl)-1,3-dimethyl-5-fluoro-1H-pyrazole-4-carboxamide, 3-(difluoro
  • the pesticide comprises fluxapyroxad, difenoconazole, and propiconazole.
  • the pesticide is water-insoluble. It is soluble in water to not more than 1 g/l, preferably not more than 200 mg/l and in particular to not more than 50 mg/l at 25°C. Using simple preliminary experiments, the skilled worker can select a pesticide with a suitable water-solubility from the above pesticide list.
  • the pesticide can have a melting point of more than 40°C, preferably more than 70°C and in particular more than 90°C.
  • the pesticide is preferably present in the concentrate in dissolved form. Using simple preliminary experiments, the skilled worker can select, from the above pesticide list, a pesticide with a suitable solubility.
  • the concentrate can comprise one or more further pesticides.
  • the further pesticide is preferably water-insoluble. Usually, it is soluble in water to not more than 1 g/l, preferably not more than 200 mg/l and in particular not more than 50 mg/l at 25°C. Using simple preliminary experiments, the skilled worker can select a pesticide with a suitable water-solubility from the above pesticide list. In an especially preferred form, the concentrate does not comprise any further pesticide.
  • the concentrate may comprise from 0.1 to 60% by weight, preferably from 1 to 25% by weight, in particular from 5 to 15% by weight, of pesticide, the basis being the total of all the pesticides present in the concentrate.
  • the emulsifiable concentrate can furthermore comprise auxiliaries conventionally used for crop protection products.
  • auxiliaries are solvents, liquid carriers, surfactants, dispersants, emulsifiers, wetters, adjuvants, solubilizers, penetrants, protective colloids, stickers, thickeners, bactericides, antifreeze agents, antifoam agents, colorants, adhesives and binders.
  • Suitable solvents and liquid carriers are organic solvents such as oils of vegetable or animal origin; alcohols, for example ethanol, propanol, butanol, cyclohexanol; glycols; ketones; esters; and their mixtures.
  • Suitable surfactants are surface-active compounds, such as anionic, cationic, nonionic and amphoteric surfactants, block polymers, polyelectrolytes, and mixtures thereof. Such surfactants can be used as emusifier, dispersant, solubilizer, wetter, penetrant, protective colloid, or auxiliary. Examples of surfactants are listed in McCutcheon's, Vol.1: Emulsifiers & Detergents, McCutcheon's Directories, Glen Rock, USA, 2008 (International Ed. or North American Ed. ).
  • Suitable anionic surfactants are alkali, alkaline earth or ammonium salts of sulfonates, sulfates, phosphates, carboxylates, and mixtures thereof.
  • sulfonates are alkylarylsulfonates, diphenylsulfonates, alpha-olefin sulfonates, lignine sulfonates, sulfonates of fatty acids and oils, sulfonates of ethoxylated alkylphenols, sulfonates of alkoxylated arylphenols, sulfonates of condensed naphthalenes, sulfonates of dodecyl- and tridecylbenzenes, sulfonates of naphthalenes and alkylnaphthalenes, sulfosuccinates or sulfosuccinamates.
  • sulfates are sulfates of fatty acids and oils, of ethoxylated alkylphenols, of alcohols, of ethoxylated alcohols, or of fatty acid esters.
  • phosphates are phosphate esters.
  • carboxylates are alkyl carboxylates, and carboxylated alcohol or alkylphenol ethoxylates.
  • Preferred anionic surfactants are sulfates and sulfonates.
  • Suitable nonionic surfactants are alkoxylates, N-subsituted fatty acid amides, amine oxides, esters, sugar-based surfactants, polymeric surfactants, and mixtures thereof.
  • alkoxylates are compounds such as alcohols, alkylphenols, amines, amides, arylphenols, fatty acids or fatty acid esters which have been alkoxylated with 1 to 50 equivalents.
  • Ethylene oxide and/or propylene oxide may be employed for the alkoxylation, preferably ethylene oxide.
  • N-subsititued fatty acid amides are fatty acid glucamides or fatty acid alkanolamides.
  • esters are fatty acid esters, glycerol esters or monoglycerides.
  • sugar-based surfactants are sorbitans, ethoxylated sorbitans, sucrose and glucose esters or alkylpolyglucosides.
  • polymeric surfactants are homo- or copolymers of vinylpyrrolidone, vinylalcohols, or vinylacetate.
  • Preferred nonionic surfactants are alkoxylates. Nonionic surfactants such as alkoxylates may also be employed as adjuvants.
  • Suitable cationic surfactants are quaternary surfactants, for example quaternary ammonium compounds with one or two hydrophobic groups, or salts of long-chain primary amines.
  • Suitable amphoteric surfactants are alkylbetains and imidazolines.
  • Suitable block polymers are block polymers of the A-B or A-B-A type comprising blocks of polyethylene oxide and polypropylene oxide, or of the A-B-C type comprising alkanol, polyethylene oxide and polypropylene oxide.
  • Suitable polyelectrolytes are polyacids or polybases, wherein polyacdis are preferred.
  • polybases are polyvinylamines or polyethyleneamines.
  • polyacids are acrylic acid copolymers, or AMPS (2-acrylamido-2-methylpropane sulfonic acid) copolymers.
  • Preferred polyelectrolyte is a copolymer, which contains in polymerized form an amide containing at least one monomer selected from N-vinyllactam, N-C 1 -C 6 alkyl acrylamide and N,N-di-C 1 -C 6 alkyl acrylamide; a poly(C 2-6 alkylene glycol) (meth)acrylate and/or a mono C 1-22 alkyl terminated poly(C 2-6 alkylene glycol) (meth)acrylate; a C 1 -C 8 alkyl (meth)acrylate; and (meth)acrylic acid.
  • More preferred polyelectrolyte is a copolymer, which contains in polymerized form an amide containing at least one monomer selected from N-vinyllactam; a mono C 1-22 alkyl terminated poly(C 2-6 alkylene glycol) (meth)acrylate; a C 1 -C 8 alkyl (meth)acrylate; and (meth)acrylic acid.
  • the polyelectrolyte is a copolymer, which contains in polymerized form 25 to 85 wt% of an amide containing at least one monomer selected from N-vinyllactam; 1 to 40 wt% of a mono C 1-22 alkyl terminated poly(C 2-6 alkylene glycol) (meth)acrylate; 5 to 50 wt% of a C 1 -C 8 alkyl (meth)acrylate; and up to 15 wt% of (meth)acrylic acid, wherein the sum of monomers equals 100 %.
  • the polyelectrolyte is a copolymer, which contains in polymerized form 30 to 85 wt% of an amide containing at least one monomer selected from N-vinyllactam; 5 to 20 wt% of a mono C 1-22 alkyl terminated poly(C 2-6 alkylene glycol) (meth)acrylate; 8 to 35 wt% of a C 1 -C 8 alkyl (meth)acrylate; and 0,5 to 10 wt% of (meth)acrylic acid, wherein the sum of monomers equals 100 %.
  • the polyelectrolyte is a copolymer, which contains in polymerized form at least one ethylenically unsaturated monomer containing sulfonic acid groups, at least one monomer selected from C 1 -C 4 alkyl (meth)acrylates, and at least one monomer selected from C 6 -C 22 alkyl (meth)acrylates.
  • the polyelectrolyte is a copolymer, which contains in polymerized form 5% to 50% by weight of at least one ethylenically unsaturated monomer containing sulfonic acid groups, 20% to 70% by weight of at least one monomer selected from C 1 -C 4 alkyl (meth)acrylates, and 5% to 30% by weight of at least one monomer selected from C 6 -C 22 alkyl (meth)acrylates, based on the total weight of the monomers.
  • the concentrate may comprise from 0.5 to 40% by weight, preferably from 2 to 30% by weight, and in particular from 5 to 25% by weight of the polyelectrolye (e.g. the polyacid, like acrylic acid copolymers, or AMPS copolymers).
  • Suitable adjuvants are compounds which have negligible or even no pesticidal activity themselves, and which improve the biological performance of the pesticide on the target. Examples are surfactants, mineral or vegetable oils, and other auxilaries. Further examples are listed by Knowles, Adjuvants and Additives, Agrow Reports DS256, T&F Informa UK, 2006, chapter 5 .
  • Suitable bactericides are bronopol and isothiazolinone derivatives such as alkylisothiazolinones and benzisothiazolinones.
  • Suitable antifreeze agents are ethylene glycol, propylene glycol, urea and glycerol.
  • Suitable antifoam agents are silicones, long-chain alcohols, and salts of fatty acids.
  • Suitable colorants e.g. in red, blue, or green
  • examples are inorganic colorants (e.g. iron oxide, titanium oxide, iron hexacyanoferrate) and organic colorants (e.g. alizarin, azo and phthalocyanine colorants).
  • the concentrate preferably comprises at least one anionic surfactant.
  • the concentrate usually comprises not less than 0.03% by weight of anionic surfactants, preferably not less than 0.1% by weight and in particular not less than 0.5% by weight.
  • the composition can comprise not more than 25% by weight of anionic surfactants, preferably not more than 10% by weight and in particular not more than 5% by weight.
  • the concentrate preferably comprises at least one nonionic surfactant (such as alkoxylates).
  • the concentrate usually comprises not less than 1% by weight of nonionic surfactants, preferably not less than 5% by weight and in particular not less than 10% by weight.
  • the composition can comprise not more than 65% by weight of nonionic surfactants, preferably not more than 45% by weight and in particular not more than 35% by weight.
  • the concentrate preferably comprises at least one alkoxylate, in particular an alkoxylated C 6 -C 22 -alcohol.
  • the concentrate usually comprises not less than 2% by weight of alkoxylates (in particular an alkoxylated C 6 -C 22 -alcohol), preferably not less than 7% by weight and in particular not less than 10% by weight.
  • the concentrate comprises a nonionic surfactant (such as alkoxylates) and an anionic surfactant (such as sulfates or sulfonates).
  • a nonionic surfactant such as alkoxylates
  • an anionic surfactant such as sulfates or sulfonates
  • the invention furthermore relates to a process for the preparation of the emulsifiable concentrate according to the invention by mixing the water-insoluble pesticide, the amide of the formula (I), the lactamide of the formula (II), and optionally the hydrocarbon.
  • the invention furthermore relates to an emulsifiable concentrate as mentioned above comprising the water-insoluble pesticides fluxapyroxad, difenoconazole, and propiconazole.
  • the concentrate may comprise further pesticides in addition to these three pesticides.
  • the emulsifiable concentrate may comprise 5 to 300 g/l (preferably 15 to 200 g/l) fluxapyroxad, 30 to 500 g/l (preferably 100 to 350 g/l) difenoconazole, and 30 to 500 g/l (preferably 100 to 350 g/l) propiconazole.
  • the emulsifiable concentrate comprising fluxapyroxad, difenoconazole, and propiconazole may further comprise auxiliaries conventionally used for crop protection products.
  • the emulsifiable concentrate comprising fluxapyroxad, difenoconazole, and propiconazole may further comprise the amide of the formula (I) and the lactamide of the formula (II).
  • the emulsifiable concentrate comprising as water-insoluble pesticides fluxapyroxad, difenoconazole, and propiconazole may have preferred features as those disclosed for the general emulsifiable concentrate comprising the water-insoluble pesticide, the amide of the formula (I) and the lactamide of the formula (II), taking into account that the emulsifiable concentrate comprising these three specific pesticides is a particular embodiment of the general one.
  • the invention furthermore relates to an emulsion obtained by mixing water and the emulsifiable concentrate according to the invention.
  • the emulsion normally arises spontaneously upon mixing.
  • the emulsion is an oil-in-water emulsion.
  • the mixing ratio of water to concentrate can be in the range of from 1000 to 1 up to 1 to 1, preferably 200 to 1 up to 3 to 1.
  • the invention furthermore relates to a method for controlling phytopathogenic fungi or undesired vegetation or for regulating the growth of plants, where the concentrate according to the invention or the emulsion according to the invention is allowed to act on the soil or on undesired plants or on the crop plants or their environment.
  • the therapeutic treatment of humans and animals is excluded from the method for controlling phytopathogenic fungi or undesired vegetation or undesired attack by insects or mites or for regulating the growth of plants.
  • the application rates of the pesticides amount to from 0.001 to 2 kg per ha, preferably from 0.005 to 2 kg per ha, especially preferably from 0.05 to 0.9 kg per ha and in particular from 0.1 to 0.75 kg per ha, depending on the nature of the desired effect.
  • amounts of active substance of from 0.1 to 1000 g, preferably from 1 to 1000 g, more preferably from 1 to 100 g and most preferably from 5 to 100 g, per 100 kg of plant propagation material (preferably seed) are generally required.
  • the amount of active substance applied depends on the kind of application area and on the desired effect. Amounts customarily applied in the protection of materials are 0.001 g to 2 kg, preferably 0.005 g to 1 kg, of active substance per cubic meter of treated material.
  • oils, wetters, adjuvants, fertilizers or micronutrients and further pesticides may be added to the emulsion in the form of a premix or optionally only shortly before use (tank mix).
  • pesticides for example herbicides, insecticides, fungicides, growth regulators, safeners
  • These agents can be admixed to the compositions according to the invention at a weight ratio of from 1:100 to 100:1, preferably from 1:10 to 10:1.
  • the user applies the composition according to the invention usually from a predosage device, a knapsack sprayer, a spray tank, a spray plane, or an irrigation system.
  • the agrochemical composition is made up with water, buffer, and/or further auxiliaries to the desired application concentration and the ready-to-use spray liquor or the agrochemical composition according to the invention is thus obtained.
  • 20 to 2000 liters, preferably 50 to 400 liters, of the ready-to-use spray liquor are applied per hectare of agricultural useful area.
  • the concentrate is highly stable to low temperatures (e.g. even below 0°C); that the pesticide does not precipitate, cream or crystallize in the concentrate at low temperatures (e.g. even below 0°C); that the pesticide does not precipitate, cream or crystallize in the emulsion obtained from the concentrate, e.g. at low temperatures (e.g. even below 0°C); that high pesticide concentrations in the concentrate can be employed; that an emulsion forms spontaneously upon dilution of the concentrate with water; that the concentrate is capable of being stored over prolonged periods; that the concentrate does not require the presence of water (e.g.
  • the concentrate forms a stable emulsion upon dilution with water; that adjuvants (such as alcohol alkoxylates) can be included in the concentrate formulations, e.g. even in high concentrations; that the pesticide in the emulsion obtained from the concentrate does not clogg any spraying filters or nozzles, e.g. at low temperatures, or when diluted with hard water.
  • adjuvants such as alcohol alkoxylates
  • Polymer A Copolymer prepared by radical polymerization, comprising a monomer mixture of 38 wt% vinylpyrrolidone, 29 wt% methyl methacrylate, 20 wt% tert-butyl acrylate, 3 wt% methacrylic acid, and 10 wt% C 16/18 alkyl terminated polyethylene glycol (25 EO) methacrylate.
  • the emulsifiable concentrates of Pesticide A were prepared by mixing the components as indicated in Table 1 (where each composition contained 10 g/l AS1 and 40 g/l NS1) and filling up to a total volume of 1.0 l with Fatty Amide A.
  • the compositions were clear solutions and are summarized in Table 1.
  • Table 1 Composition (all data in g/l) A B C D E NS3 100 100 100 200 150 NS2 100 100 100 100 50 50 50 Lactamide A 50 50 100 50 50 Polymer A 75 50 50 100 100 Hydrocarbon 200 100 100 100 100 100 Active Solubility Dissolved Dissolved Dissolved Dissolved Applicability Free Free Free Free Cold Stability Stable Stable Stable Stable Stable Stable Stable
  • each prepared EC formulation was placed in a refrigerator at -10 °C. After 3 days storage in the refrigerator, the formulations were seeded with the respective pesticide crystals (less than 0.1 g/l). Twelve days after seeding the samples were observed for the crystallization of pesticide. Samples which did not show any crystals other than the added seed crystals were marked “Stable”. Samples which showed crystals other than the added seed crystals were marked "Crystals”.
  • the test machine was a hydraulic sprayer with a 195 l tank, a four-piston membrane pump (at 3 bar pressure) and a spraying lance with 6 standard nozzles (type: LU 90-03).
  • Nozzle filtersused were four mesh filters (25, 50, 60, and 80 mesh), a 60-mesh mesh filter with integrated seal, and a 25-mesh slot filter.
  • the suction filter and the pressure filter were each 50-mesh mesh filters.
  • the tank was first filled with 75 l of water and thereafter one liter of an emulsifiable concentrate.
  • the mixture was mixed with a piston pump (stirring intensity: 45 l/min) and subsequently the tank was filled up with a further 75 l of water. After pumped circulation for 120 minutes (stirring 5 intensity: 45 l/min) of the product mixture, the spray solution was sprayed out of the tank through the nozzles. During the test, the temperature of the spray mixture in the tank was kept constant at between 5 and 10°C in order to simulate cold well water. The delivery test was repeated 4 times without cleaning the instruments between each application.
  • the emulsifiable concentrates of Pesticide A were prepared by mixing the components as indicated in Table 2 (where each composition contained 10 g/l AS1, 40 g/l NS1, 50 g/l NS2, 200 g/l NS3, and 100 g/l Polymer A).
  • Sample D corresponds to Sample D of Example 1. The samples were tested for "Active Solubility", “Applicability” and “Cold Stability” as described in Example 1.
  • Table 2 Composition (all data in g/l) D Comp A a) Comp B a) COmp C a) Lactamide A 50 - Ad 1.0 L 50 Fatty Amide A Ad 1,0 L Ad 1,0 L - - Hydrocarbon 100 100 100 Ad 1.0 L Active Solubility Dissolved Dissolved Crystals Applicability Free Free Clogged - Cold Stability Stable Crystals Stable - a) not according to the invention
  • the emulsifiable concentrates of Pesticide A (each 100 g/l), fluxapyroxad (each 50 g/l), and pyraclostrobin (each 100 g/l) were prepared by mixing the components as indicated in Table 3 (where each composition contained 10 g/l AS1 and 40 g/l NS1). The samples were tested for "Active Solubility", “Applicability” and “Cold Stability” as described in Example 1.
  • Table 3 Composition (all data in g/l) A Comp A a) Comp B a) NS3 150 150 150 NS2 50 50 50 50 50 Lactamide A 50 - 50 Fatty Amide A Ad 1.0 L Ad 1.0 L - Hydrocarbon 100 100 Ad 1.0 L Active Solubility Dissolved Dissolved Crystals Applicability Free Free - Cold Stability Stable Crystals - a) not according to the invention
  • the emulsifiable concentrates of fluxapyroxad (each 30 g/l), pyraclostrobin (each 200 g/l) and propiconazole (each 125 g/l) were prepared by mixing the components and filling up to a total volume of 1,0 l with Hydrocarbon as indicated in Table 4. The samples were tested for "Active Solubility", “Applicability” and “Cold Stability” as described in Example 1.
  • Table 4 Composition (all data in g/l) A B C D Lactamide A 50 50 50 50 Fatty Amide A 150 150 150 150 AS1 10 10 - - NS1 40 40 - - NS2 150 150 100 - NS3 150 150 100 150 NS4 - - 100 100 NS5 - - 100 100 Applicability Free Free Free Free Cold Stability Stable Stable Stable Stable Active Solubility Dissolved Dissolved Dissolved Dissolved Dissolved Dissolved Dissolved Dissolved Dissolved
  • the emulsifiable concentrates of fluxapyroxad (each 67 g/l), pyraclostrobin (each 133 g/l) and difenoconazole (each 100 g/l) were prepared by mixing the components as indicated in Table 5. The samples were tested for "Active Solubility”, “Applicability” and “Cold Stability” as described in Example 1.
  • Table 5 Composition (all data in g/l) A B Lactamide A 50 50 Fatty Amide A 200 Ad 1.0 L Hydrocarbon Ad 1,0 L 150 Polymer A - 75 NS2 - 200 NS3 200 - NS4 50 30 NS5 - 40 AS2 50 - Applicability Free Free Cold Stability Stable Stable Active Solubility Dissolved Dissolved
  • the emulsifiable concentrates of Pesticide A (each 100 g/l) and propiconazole (each 125 g/l) were prepared by mixing the components and filling up to a total volume of 1.0 L with Hydrocarbon as indicated in Table 6. The samples were tested for "Active Solubility", “Applicability” and "Cold Stability” as described in Example 1.
  • Table 6 Composition (all data in g/l) A Lactamide A 50 Fatty Amide A 150 NS1 40 NS3 200 AS1 10 Applicability Free Cold Stability Stable Active Solubility Dissolved
  • the emulsifiable concentrate of fluxapyroxad (40 g/l), pyraclostrobin (266,6 g/l) and propiconazole (166,6 g/l) was prepared by mixing the components as indicated in Table 7 and 75 g/l Polymer A, and filling up to a total volume of 1,0 l with Hydrocarbon.
  • the compositions are summarized in Table 7. The samples were tested for "Applicability" and "Cold Stability" as described in Example 1.
  • Table 7 Composition (all data in g/l) A NS2 200 NS4 30 NS5 40 Lactamide A 50 Fatty Amide A 175 Applicability Free Cold Stability Stable
  • the emulsifiable concentrate of fluxapyroxad (60 g/l), difenoconazole (250 g/l) and propiconazole (250 g/l) was prepared by mixing the components and filling up to a total volume of 1.0 l with Hydrocarbon.
  • the compositions are summarized in Table 8. The samples were tested for "Applicability” and "Cold Stability" as described in Example 1.
  • Table 8 Composition (all data in g/l) (not according to the invention) A NS2 50 NS4 30 NS5 40 Lactamide A 50 Fatty Amide A 150 Applicability Free Cold Stability Stable

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  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Pest Control & Pesticides (AREA)
  • Plant Pathology (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • Agronomy & Crop Science (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Toxicology (AREA)
  • Chemical & Material Sciences (AREA)
  • Dispersion Chemistry (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Claims (14)

  1. Emulsionskonzentrat, umfassend ein wasserunlösliches Pestizid, wobei das Pestizid bei 25°C zu nicht mehr als 1 g/l in Wasser löslich ist,
    ein Amid der Formel (I)

            R1-C(O)N(R2)2     (I),

    wobei R1 für C5-C19-Alkyl steht und R2 für Methyl, Ethyl, Propyl, Butyl oder Mischungen davon steht, und
    ein Lactamid der Formel (II)

            H3C-CH(OH)-C(O)N(R3)2     (II),

    wobei R3 für Methyl, Ethyl, Propyl, Butyl oder Mischungen davon steht,
    wobei das Konzentrat Folgendes umfasst:
    15 Gew.-% bis 65 Gew.-% des Amids der Formel (I) und 1 Gew.-% bis 30 Gew.-% des Lactamids der Formel (II), wobei die Summe der Mengen dieser Komponenten 16 bis 90 Gew.-% beträgt.
  2. Konzentrat nach Anspruch 1, wobei R1 für C8-C14-Alkyl steht.
  3. Konzentrat nach Anspruch 1 oder 2, wobei R1 für C7-C13-Alkyl steht.
  4. Konzentrat nach einem der Ansprüche 1 bis 3, wobei R2 in Formel (I) für Methyl steht.
  5. Konzentrat nach einem der Ansprüche 1 bis 4, wobei R3 in Formel (II) für Methyl steht.
  6. Konzentrat nach einem der Ansprüche 1 bis 5, welches weiterhin einen Kohlenwasserstoff umfasst.
  7. Konzentrat nach Anspruch 6, welches 2 bis 45 Gew.-% an Kohlenwasserstoff umfasst.
  8. Konzentrat nach einem der Ansprüche 1 bis 7, wobei das Gewichtsverhältnis des Amids der Formel (I) zum Lactamid der Formel (II) im Bereich von 1:2 bis 15:1 liegt.
  9. Konzentrat nach einem der Ansprüche 1 bis 7, wobei das Gewichtsverhältnis des Amids der Formel (I) zum Lactamid der Formel (II) im Bereich von 1:1 bis 13:1 liegt.
  10. Konzentrat nach Anspruch 1, umfassend 15 bis 65 Gew.-% an Amid der Formel (I), 1 bis 30 Gew.-% an Lactamid der Formel (II) und 5 bis 40 Gew.-% eines Kohlenwasserstoffs, wobei die Summe der Mengen dieser Komponenten 16 bis 90 Gew.-% beträgt.
  11. Emulsionskonzentrat nach Anspruch 1, umfassend die wasserunlöslichen Pestizide Fluxapyroxad, Difenoconazol und Propiconazol.
  12. Verfahren zur Herstellung des Konzentrats nach einem der Ansprüche 1 bis 10 durch Mischen des wasserunlöslichen Pestizids, des Amids der Formel (I), des Lactamids der Formel (II) und gegebenenfalls des Kohlenwasserstoffs.
  13. Emulsion, erhalten durch Mischen von Wasser mit dem wie in einem der Ansprüche 1 bis 10 definierten Emulsionskonzentrat.
  14. Verfahren zur Bekämpfung phytopathogener Pilze oder unerwünschten Pflanzenwuchses oder zur Regulierung des Wachstums von Pflanzen, bei dem man das Konzentrat nach einem der Ansprüche 1 bis 10 oder die Emulsion nach Anspruch 13 auf den Boden oder auf die unerwünschten Pflanzen oder auf die Kulturpflanzen oder ihre Umgebung einwirken lässt, wobei die therapeutische Behandlung von Menschen und Tieren von diesem Verfahren ausgeschlossen ist.
EP15704994.1A 2014-02-14 2015-02-10 Emulgierbares konzentrat mit pestizid, fettsäureamid und lactamid Active EP3104700B1 (de)

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Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PL3104700T3 (pl) 2014-02-14 2019-03-29 BASF Agro B.V. Koncentrat do sporządzania emulsji wodnej zawierający pestycyd, amid tłuszczowy i laktamid
EP4038038A1 (de) * 2019-09-30 2022-08-10 Basf Se Stabile wässrige düngerzusammensetzungen und landwirtschaftlich aktive verbindung
WO2024201452A1 (en) * 2023-03-24 2024-10-03 Adama Makhteshim Ltd. Liquid homogeneous agrochemical composition of insecticides

Family Cites Families (37)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BG48681A3 (bg) 1982-12-14 1991-04-15 Ciba - Geigy Ag Фунгицидно средство
DE3484968D1 (de) 1983-05-19 1991-10-02 Ciba Geigy Ag Verfahren zur herstellung von 1-triazolylethylether-derivaten, sowie mikrobizide mittel enthaltende neue 1-triazolyl-phenoxyphenylethylether-derivate als wirkstoffe und deren verwendung.
ES2016660B3 (es) 1987-01-21 1990-11-16 Ciba-Geigy Ag Agente microbicida.
DE4003180A1 (de) 1990-02-03 1991-08-08 Bayer Ag Halogenallyl-azolyl-derivate
EP2043446A2 (de) 2006-02-08 2009-04-08 Phibro-Tech Inc. Biozide azol-emulsionskonzentrate mit hohem wirkstoffgehalt
GB0605780D0 (en) 2006-03-22 2006-05-03 Syngenta Ltd Formulations
GB0716593D0 (en) 2007-08-24 2007-10-03 Syngenta Ltd Improvements in or relating to organic compounds
GB0716592D0 (en) * 2007-08-24 2007-10-03 Syngenta Ltd Improvements in or relating to organic compounds
WO2011082162A1 (en) 2009-12-29 2011-07-07 Syngenta Participations Ag Pesticidal composition
EP2523658B1 (de) * 2010-01-11 2018-05-30 ISP Investments LLC Matrixzusammensetzung zur verabreichung hydrophober wirkstoffe
PL2380954T3 (pl) * 2010-04-22 2013-08-30 Cognis Ip Man Gmbh Kompozycje rozpuszczalnikowe
US20120142676A1 (en) 2010-08-18 2012-06-07 Gaik-Lean Chee Oxathiazine and dithiine oxides as inhibitors of sulfhydryl-dependent biomolecules
WO2013007767A1 (en) 2011-07-13 2013-01-17 Basf Se Fungicidal substituted 2-[2-halogenalkyl-4-(phenoxy)-phenyl]-1-[1,2,4]triazol-1-yl-ethanol compounds
JP2014520833A (ja) 2011-07-15 2014-08-25 ビーエーエスエフ ソシエタス・ヨーロピア 殺菌性フェニルアルキル−置換２−［２−クロロ−４−（４−クロロ−フェノキシ）−フェニル］−１−［１，２，４］トリアゾール−１−イル−エタノール化合物
CN103648281B (zh) 2011-07-15 2016-05-25 巴斯夫欧洲公司 杀真菌的烷基取代的2-[2-氯-4-(4-氯苯氧基)苯基]-1-[1,2,4]三唑-1-基乙醇化合物
JP2014520831A (ja) 2011-07-15 2014-08-25 ビーエーエスエフ ソシエタス・ヨーロピア 殺菌性アルキル−およびアリール−置換２−［２−クロロ−４−（ジハロ−フェノキシ）−フェニル］−１−［１，２，４］トリアゾール−１−イル−エタノール化合物
EP2744791B1 (de) 2011-08-15 2015-10-28 Basf Se Fungizide substituierte 1-{2-[2-halo-4-(4-halogen-phenoxy-)phenyl-]2-alkoxy-3-methyl-butyl}-1h-[1,2,4-]triazol-verbindungen
JP2014525404A (ja) 2011-08-15 2014-09-29 ビーエーエスエフ ソシエタス・ヨーロピア 殺菌性置換１−｛２−［２−ハロ−４−（４−ハロゲン−フェノキシ）−フェニル］−２−アルキニルオキシ−エチル｝−１ｈ−［１，２，４］トリアゾール化合物
KR20140054235A (ko) 2011-08-15 2014-05-08 바스프 에스이 살진균 치환된 1-｛2-［2-할로-4-(4-할로겐-페녹시)-페닐］-2-알콕시-2-시클릴-에틸｝-1h-［1,2,4］트리아졸 화합물
JP2014525407A (ja) 2011-08-15 2014-09-29 ビーエーエスエフ ソシエタス・ヨーロピア 殺菌性置換１−｛２−［２−ハロ−４−（４−ハロゲン−フェノキシ）−フェニル］−２−アルコキシ−２−アルキニル／アルケニル−エチル｝−１ｈ−［１，２，４］トリアゾール化合物
MX2014000511A (es) 2011-08-15 2014-02-19 Basf Se Compuestos fungicidas de 1-{2-[2-halo-4-(4-halogen-fenoxi)-fenil]- 2-etoxi-etil}-1h-[1,2,4]triazol sustituidos.
WO2013024081A1 (en) 2011-08-15 2013-02-21 Basf Se Fungicidal substituted 1-{2-[2-halo-4-(4-halogen-phenoxy)-phenyl]-2-alkoxy-hexyl}-1h [1,2,4]triazole compounds
WO2013024082A1 (en) 2011-08-15 2013-02-21 Basf Se Fungicidal substituted 1-{2-cyclyloxy-2-[2-halo-4-(4-halogen-phenoxy)-phenyl]-ethyl}-1h-[1,2,4]triazole compounds
EP2790500B1 (de) 2011-12-14 2015-11-25 Basf Se Emulgierbares konzentrat mit einem pestizid, einem amid, einem carbonat und kohlenwasserstoff
CN104202978B (zh) 2012-04-04 2016-06-22 巴斯夫欧洲公司 包含乙烯基内酰胺、n-烷基丙烯酰胺和(甲基)丙烯酸烷基酯的共聚物的农业配制剂
HUE035342T2 (en) 2012-04-04 2018-05-02 Basf Se Agroforulation with an amide, polyalkylene glycol (meth) acrylate and alkyl (meth) acrylate copolymer
BR112014024417B1 (pt) 2012-04-16 2021-08-17 Basf Se Composição, processo para preparar a composição e método para controlar fungos fitopatogênicos
CN103385256A (zh) * 2012-05-07 2013-11-13 陕西韦尔奇作物保护有限公司 一种含氟唑菌酰胺与三唑类的增效杀菌组合物
EP2861065B1 (de) 2012-06-18 2017-03-15 Basf Se Landwirtschaftliche formulierungen mit lactonbasiertem alkoxylat
WO2014128009A1 (en) 2013-02-19 2014-08-28 Basf Se Aqueous agrochemical composition comprising a pesticide in suspended form, a dispersant, and an ionic liquid
KR20150128838A (ko) 2013-03-07 2015-11-18 바스프 에스이 피리메타닐 및 선택된 디티인 테트라카르복시미드의 공동-결정
JP2016515107A (ja) 2013-03-13 2016-05-26 ビーエーエスエフ ソシエタス・ヨーロピアＢａｓｆ Ｓｅ 殺有害生物剤、安息香酸アルキル及び脂肪酸アミドを含む乳化性濃縮物
JP2016520422A (ja) 2013-05-06 2016-07-14 ビーエーエスエフ ソシエタス・ヨーロピアＢａｓｆ Ｓｅ 疎水性の異なるポロキサマーの混合物を可溶化剤として含む難水溶性活性成分の水性製剤
EP3019013B1 (de) 2013-07-08 2020-12-23 BASF Agro B.V. Zusammensetzungen enthaltend eine triazolverbindung und ein biopestizid
JP2016540072A (ja) 2013-11-15 2016-12-22 ビーエーエスエフ ソシエタス・ヨーロピアＢａｓｆ Ｓｅ 活性剤と、ｎ−ビニルラクタム、ビニルエステル及びアルコールアルコキシレートから製造されたグラフトコポリマーとを含む組成物
PL3104700T3 (pl) 2014-02-14 2019-03-29 BASF Agro B.V. Koncentrat do sporządzania emulsji wodnej zawierający pestycyd, amid tłuszczowy i laktamid
US20170049097A1 (en) 2014-02-14 2017-02-23 BASF Agro B.V. Emulsifiable Concentrate Comprising Pesticide, Alkyl Lactate, and Lactamide

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
None *

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US10383334B2 (en) 2019-08-20
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